Langerhans cell sarcoma

Dendritic cell neoplasms are classified by the World Health Organization as follows:[4]

• Langerhans cell histiocytosis
• Langerhans cell sarcoma
• Interdigitating dendritic cell sarcoma/tumor
• Follicular dendritic cell sarcoma/tumor
• Dendritic cell sarcoma

The exact incidence of LCS is unknown due to the rarity of the condition. The related condition, Langerhans Cell Histiocytosis (LCH) is estimated to have an incidence of around 5 cases per 1 million people per year.[5] In one review of Japanese patients with confirmed LCS, patients were a median age of 41 years.[5] Patients were twice as likely to be female than male.[5] In another systematic review, the median age of presentation was 50 years, but with a slight predilection for males.[3]

Throughout the body in locations such as mucous membranes, skin, lymph nodes, thymus, and spleen are cells known as antigen-presenting cells. These cells are surveillance cells that take foreign antigens and present them to antigen-processing cells, such as T-cells, protecting the body from potential harm.[6][7] Antigen-presenting cells are also termed Dendritic cells, of which Langerhans cells are a subtype.[6] There are four main types that make up the structure and functions of lymphoid tissue, such as lymph nodes and splenic tissue.[4] By definition, Langerhans Cell Sarcoma (LCS) is a cancerous disease caused by the uncontrolled overproliferation of Langerhans cells.[5]

Because Langerhans cells are most commonly found in the mucosa and the skin, LCS is thought to usually begin here with further spread to other areas of the body via the lymphatic system.[3]

Langerhans cell sarcoma can occur de novo, or can occur as a malignant transformation of Langerhans cell histiocytosis.[3][8]

The related condition, LCH, presents with various clinical features depending on the bodily organs involved.[5] LCS shares most of these clinical presentations. Most commonly, these patients will present with generalized signs and symptoms such as fever and weight loss.[5] Blood tests will commonly show pancytopenia, an overall reduction in blood cell counts.[5] Additionally, these patients may display lymphadenopathy, hepatosplenomegaly, skin lesions, bone lesions, and lung lesions.[5] Most common site presentations are the skin and lymphatics.[6][3] Other common sites of involvement include the lung, liver, and spleen.[3]

LCS will present with a varied gross appearance. When involving the skin, LCS will present as a patches of erythema, with nodules and ulceration present as well.[9] Skin lesions will most commonly involve the trunk, scalp, and legs.[9] Tumor size may range from 1-6 cm, but may be larger. Usually the tumor is well circumscribed with a surface covered in small nodules or protuberances. Most are of a solid consistency and are of a pink, white, or tan color. LCS tumors may present with much larger sizes and aggressive features, even causing some bleeding and necrosis of the surrounding tissue.[4]

Diagnosis of Langerhans Cell Sarcoma is predominantly a pathologic diagnosis. Cells from these tumor samples will display features characteristic of Langerhans cells, but with additional signs of malignancy, such as increased mitoses, cellular atypia, and pleomorphic nuclei.[5]

CD-207 is a cellular marker associated with Birbeck granules than can be used for confirmation of cell type.[5] LCS will also stain positive for CD-68, CD-68R, CD-21, CD-35, S-100, CD1a, lysozyme, HLA-DR, CD4, fascin, Factor XIIIa, and cyclin D1, which are cellular markers typically used in the characterization of various pathology specimens.[4][5][6] Positive staining with CD1a and S-100 are required for diagnosis of LCS.[4] Positive staining with CD-207 (Langerin) is an additional confirmation marker of malignancy in LCS.[6][3][9] Other cellular markers have been reported to be positive in LCS, but have are not as routinely used.[5]

Histologically, Langerhans cells characteristically display Birbeck granules and nuclei with a longitudinal groove.[5][6] Birbeck granules are currently a poorly understood cellular structure, but are commonly used for cell-type identification.[10] Previously, the presence of Birbeck granules was necessary for diagnosis, but this is no longer considered diagnostic.[6]

Currently, there appears to be no relation of LCS with chromosomal abnormalities.[5]

The diagnosis of LCS can be difficult, especially due to its rarity. It has previously been mistaken with metastatic melanoma and metastatic large-cell carcinoma.[8]

Treatment for this rare disease consists of a variety of approaches, with none displaying any increased efficacy over another.[4] There are currently three broad treatment strategies for LCS: surgery, chemotherapy, and combination with radiation therapy.[3] When the LCS tumor is readily accessible, the best treatment method is usually surgical removal.[4] There is, however, an observed increased risk of tumor relapse following surgical resection.[4] Both chemotherapy and radiation therapy are useful as treatments, either as monotherapy or in conjunction with other treatments.[6][3] Chemotherapy is currently the most common treatment method, either alone or in combination.[3] The most common chemotherapeutic regimen consisted of cyclophosphamide, doxorubicin, vincristine, and prednisolone (otherwise known as CHOP therapy).[3] Other common chemotherapeutic regimens include MAID (mesna, doxorubicin, ifosfamide, and dacarbazine), ESHAP (etoposide, carboplatin, cytarabine, and methylprednisolone), EPIG (etoposide, cisplatin, ifosfamide, mesna, and gemcitabine), and AIM (doxorubicin, ifosfamide, and mesna).[8] Other regimens have been used with mixed levels of success.[3] In an effort to prevent recurrence, sometimes combination therapy is used. Following surgical resection, additional radiation therapy or chemotherapy may be performed to prevent relapse.[4] Patients receiving combined chemotherapy and radiation therapy has only shown limited benefit.[4]

There are a variety of other therapies under research with varying levels of reported success. These include high-dose chemotherapy, bone marrow transplants, and somatostatin analogues.[4][3]

When there is only one site of LCS involvement, monotherapy may be sufficient treatment. But when the disease has multiple sites or has metastasized, combination therapy will be necessary to achieve any level of adequate treatment.[6]

Overall prognosis of patients with LCS depends heavily on the bodily organ involved and the extent of involvement of the tumor.[5] Organs associated with a poor prognosis include the liver, lungs, and bone marrow.[5] In patients with a single site of involvement, survivability tends to be very favorable.[6] However, those with multi-organ involvement have a mortality rate of 50-66%.[5] One systematic review calculated the disease-specific survival as 27.2 months, or 58% at one year.[3] One group found the death rate to be 50% in patients with LCS, compared to 31% in patients who had the related condition LCH.[1] Survivability decreases dramatically with increased disease burden and spread.[3] LCS may be associated with other malignancies as well, such as follicular lymphoma, adenocarcinoma, and germ cell tumors.[4] Evidence of metastatic disease or relapse from a previously treated LCS usually signifies a worsened prognosis.[4] Treatment of these metastatic lesions or relapsed tumors may improve the patient's prognosis, but there is limited evidence as to a preferred therapy.[4]

• Langerhans cell histiocytosis
• Sarcoma